Canon USA, Inc. - FDA 510(k) Cleared Devices
48
Total
48
Cleared
0
Denied
Canon USA, Inc. has 48 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 48 cleared submissions from 1984 to 2009. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Canon USA, Inc. Filter by specialty or product code using the sidebar.
48 devices
Cleared
Mar 24, 2009
DIGITAL RADIOGRAPHY CXDI-40G COMPACT
Radiology
15d
Cleared
Dec 15, 2003
PACS SOFTWARE SOLUTION 2003
Radiology
27d
Cleared
Jun 11, 2003
CANON INC., DIGITAL RADIOGRAPHY, MODEL CXDI-40C
Radiology
15d
Cleared
Jun 06, 2003
CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGI
Ophthalmic
10d
Cleared
Nov 22, 2002
CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40G
Radiology
14d
Cleared
Nov 05, 2002
DR-ER VERFSION OF CANON X-RAY DIGITAL CAMERAS
Radiology
11d
Cleared
Jan 02, 2002
CANON X-RAY DIGITAL CAMERA, MODEL CXDI-31
Radiology
398d
Cleared
Jun 21, 2000
CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100
Ophthalmic
323d
Cleared
Oct 13, 1999
CANON X-RAY DIGITAL CAMERA, MODEL CXDI-22
Radiology
75d
Cleared
Nov 04, 1998
CANON X-RAY DIGITAL CAMERA CXDI-11
Radiology
187d
Cleared
May 06, 1998
NON-MYDRIATIC RETINAL CAMERA, MODEL CR6-45NM
Ophthalmic
103d
Cleared
Mar 03, 1997
CANON TX-10 TONOMETER
Ophthalmic
208d
Looking for a specific device from Canon USA, Inc.? Search by device name or K-number.
Search all Canon USA, Inc. devices